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2013-02-12Zeitschriftenartikel DOI: 10.1371/journal.pmed.1001387
Whole Genome Sequencing versus Traditional Genotyping for Investigation of a Mycobacterium tuberculosis Outbreak: A Longitudinal Molecular Epidemiological Study
dc.contributor.authorRoetzer, Andreas
dc.contributor.authorDiel, Roland
dc.contributor.authorKohl, Thomas A.
dc.contributor.authorRückert, Christian
dc.contributor.authorNübel, Ulrich
dc.contributor.authorBlom, Jochen
dc.contributor.authorWirth, Thierry
dc.contributor.authorJaenicke, Sebastian
dc.contributor.authorSchuback, Sieglinde
dc.contributor.authorRüsch-Gerdes, Sabine
dc.contributor.authorSupply, Philip
dc.contributor.authorKalinowski, Jörn
dc.contributor.authorNiemann, Stefan
dc.date.accessioned2018-05-07T16:18:01Z
dc.date.available2018-05-07T16:18:01Z
dc.date.created2013-03-26
dc.date.issued2013-02-12none
dc.identifier.otherhttp://edoc.rki.de/oa/articles/renLE5Sn7PAuM/PDF/22QD7ZyRDAL2Y.pdf
dc.identifier.urihttp://edoc.rki.de/176904/1428
dc.description.abstractBackground: Understanding Mycobacterium tuberculosis (Mtb) transmission is essential to guide efficient tuberculosis control strategies. Traditional strain typing lacks sufficient discriminatory power to resolve large outbreaks. Here, we tested the potential of using next generation genome sequencing for identification of outbreak-related transmission chains. Methods and Findings: During long-term (1997 to 2010) prospective population-based molecular epidemiological surveillance comprising a total of 2,301 patients, we identified a large outbreak caused by an Mtb strain of the Haarlem lineage. The main performance outcome measure of whole genome sequencing (WGS) analyses was the degree of correlation of the WGS analyses with contact tracing data and the spatio-temporal distribution of the outbreak cases. WGS analyses of the 86 isolates revealed 85 single nucleotide polymorphisms (SNPs), subdividing the outbreak into seven genome clusters (two to 24 isolates each), plus 36 unique SNP profiles. WGS results showed that the first outbreak isolates detected in 1997 were falsely clustered by classical genotyping. In 1998, one clone (termed “Hamburg clone”) started expanding, apparently independently from differences in the social environment of early cases. Genome-based clustering patterns were in better accordance with contact tracing data and the geographical distribution of the cases than clustering patterns based on classical genotyping. A maximum of three SNPs were identified in eight confirmed human-to-human transmission chains, involving 31 patients. We estimated the Mtb genome evolutionary rate at 0.4 mutations per genome per year. This rate suggests that Mtb grows in its natural host with a doubling time of approximately 22 h (400 generations per year). Based on the genome variation discovered, emergence of the Hamburg clone was dated back to a period between 1993 and 1997, hence shortly before the discovery of the outbreak through epidemiological surveillance. Conclusions: Our findings suggest that WGS is superior to conventional genotyping for Mtb pathogen tracing and investigating micro-epidemics. WGS provides a measure of Mtb genome evolution over time in its natural host context.eng
dc.language.isoeng
dc.publisherRobert Koch-Institut, Infektionskrankheiten / Erreger
dc.subject.ddc610 Medizin
dc.titleWhole Genome Sequencing versus Traditional Genotyping for Investigation of a Mycobacterium tuberculosis Outbreak: A Longitudinal Molecular Epidemiological Study
dc.typeperiodicalPart
dc.identifier.urnurn:nbn:de:0257-10029725
dc.identifier.doi10.1371/journal.pmed.1001387
dc.identifier.doihttp://dx.doi.org/10.25646/1353
local.edoc.container-titlePLoS Medicine
local.edoc.container-textRoetzer, A., Diel, R., Kohl, T.A., Rückert, C., Nübel, U., Blom, J., Wirth, T., Jaenicke, S., Schuback, S., Rüsch-Gerdes, S., Supply, P., Kalinowski, J., Niemann, S. Whole Genome Sequencing versus Traditional Genotyping for Investigation of a Mycobacterium tuberculosis Outbreak: A Longitudinal Molecular Epidemiological Study (2013) PLoS Medicine, 10 (2), art. no. e1001387.
local.edoc.fp-subtypeArtikel
local.edoc.type-nameZeitschriftenartikel
local.edoc.container-typeperiodical
local.edoc.container-type-nameZeitschrift
local.edoc.container-urlhttp://www.plosmedicine.org/article/info%3Adoi%2F10.1371%2Fjournal.pmed.1001387
local.edoc.container-publisher-namePublic Library of Science
local.edoc.container-volume10
local.edoc.container-issue2
local.edoc.container-year2013

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